Variant report

Variant	esv1842334
Chromosome Location	chr7:6683454-6694679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:550)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
3	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
4	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
5	CHD2	chr7:6688733-6688788	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr7:6685100-6685250	MCF-7	breast:	n/a	n/a
7	CTCF	chr7:6688006-6688143	MCF-7	breast:	n/a	n/a
8	CTCF	chr7:6688038-6688147	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:6687900-6688050	HMEC	breast:	n/a	n/a
10	CTCF	chr7:6687960-6688110	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr7:6688074-6688083	MCF-7	breast:	n/a	n/a
12	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
13	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
14	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
15	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
16	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
17	MYC	chr7:6687405-6687481	MCF-7	breast:	n/a	n/a
18	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
19	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
20	PAX5	chr7:6693715-6694061	GM12878	blood:	n/a	chr7:6693933-6693952
21	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
22	PAX5	chr7:6693823-6694038	GM12892	blood:	n/a	chr7:6693933-6693952
23	PAX5	chr7:6692203-6692749	GM12878	blood:	n/a	n/a
24	PAX5	chr7:6693471-6694164	GM12892	blood:	n/a	chr7:6693933-6693952
25	PAX5	chr7:6693740-6694153	GM12878	blood:	n/a	chr7:6693933-6693952
26	PAX5	chr7:6692282-6692683	GM12891	blood:	n/a	n/a
27	PAX5	chr7:6693543-6694257	GM12878	blood:	n/a	chr7:6693933-6693952
28	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952
29	PAX5	chr7:6692099-6692801	GM12892	blood:	n/a	n/a
30	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
31	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
32	PBX3	chr7:6693289-6693652	GM12878	blood:	n/a	n/a
33	PBX3	chr7:6693877-6694030	GM12878	blood:	n/a	n/a
34	POLR2A	chr7:6686541-6686905	GM12892	blood:	n/a	n/a
35	POLR2A	chr7:6685946-6686167	K562	blood:	n/a	n/a
36	POLR2A	chr7:6679104-6684327	K562	blood:	n/a	n/a
37	POLR2A	chr7:6687682-6687986	K562	blood:	n/a	n/a
38	POLR2A	chr7:6689283-6689778	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:6694434-6694889	K562	blood:	n/a	n/a
40	POLR2A	chr7:6693515-6693701	MCF-7	breast:	n/a	n/a
41	POLR2A	chr7:6692197-6692397	K562	blood:	n/a	n/a
42	POLR2A	chr7:6693762-6693972	K562	blood:	n/a	n/a
43	POLR2A	chr7:6690246-6690251	MCF-7	breast:	n/a	n/a
44	POLR2A	chr7:6686531-6686729	ProgFib	skin:	n/a	n/a
45	POLR2A	chr7:6683861-6684268	GM12892	blood:	n/a	n/a
46	POLR2A	chr7:6692412-6692572	K562	blood:	n/a	n/a
47	POLR2A	chr7:6688660-6688773	K562	blood:	n/a	n/a
48	POLR2A	chr7:6688411-6689172	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:6693197-6693474	K562	blood:	n/a	n/a
50	POLR2A	chr7:6683188-6683512	GM12892	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6694373-6694423	HRE	kidney:	n/a
2	chr7:6694373-6694423	HRE	kidney:	n/a
3	chr7:6692873-6692923	GM12891	blood:	n/a
4	chr7:6693030-6693080	HEEpiC	esophagus:	n/a
5	chr7:6694373-6694423	AG09319	gingival:	n/a
6	chr7:6691949-6691999	NHDF-neo	bronchial:	n/a
7	chr7:6694373-6694423	HRCEpiC	kidney:	n/a
8	chr7:6689218-6689268	SKMC	muscle:	n/a
9	chr7:6691949-6691999	NT2-D1	testis:	n/a
10	chr7:6693030-6693080	GM12878	blood:	n/a
11	chr7:6693838-6693888	NB4	blood:	n/a
12	chr7:6691949-6691999	AG09319	gingival:	n/a
13	chr7:6692873-6692923	SK-N-SH_RA	brain:	n/a
14	chr7:6690313-6690363	HUVEC	blood vessel:	n/a
15	chr7:6692873-6692923	HL-60	blood:	n/a
16	chr7:6693334-6693384	NHBE	bronchial:	n/a
17	chr7:6693334-6693384	NB4	blood:	n/a
18	chr7:6691949-6691999	GM06990	blood:	n/a
19	chr7:6693334-6693384	HEK293	kidney:	embryo
20	chr7:6693838-6693888	PFSK-1	brain:	n/a
21	chr7:6694373-6694423	HIPEpiC	eye:	n/a
22	chr7:6693030-6693080	Hela-S3	cervix:	n/a
23	chr7:6692445-6692495	Hepatocyte	liver:	n/a
24	chr7:6692445-6692495	GM12878	blood:	n/a
25	chr7:6691949-6691999	SK-N-SH_RA	brain:	n/a
26	chr7:6693030-6693080	HCPEpiC	choroid plexus:	n/a
27	chr7:6694373-6694423	AG04450	lung:	fetal
28	chr7:6689218-6689268	H1-hESC	embryonic stem cell:	embryo
29	chr7:6694373-6694423	U87	brain:	n/a
30	chr7:6690313-6690363	LNCaP	prostate:	n/a
31	chr7:6692873-6692923	NH-A	brain:	n/a
32	chr7:6689218-6689268	HNPCEpiC	eye:	n/a
33	chr7:6689218-6689268	NT2-D1	testis:	n/a
34	chr7:6690313-6690363	SKMC	muscle:	n/a
35	chr7:6690313-6690363	NB4	blood:	n/a
36	chr7:6691949-6691999	SK-N-MC	brain:	n/a
37	chr7:6692445-6692495	HEK293	kidney:	embryo
38	chr7:6690313-6690363	HL-60	blood:	n/a
39	chr7:6693030-6693080	PFSK-1	brain:	n/a
40	chr7:6692873-6692923	PANC-1	pancreas:	n/a
41	chr7:6693838-6693888	AG04450	lung:	fetal
42	chr7:6693334-6693384	GM12892	blood:	n/a
43	chr7:6693334-6693384	HCM	heart:	n/a
44	chr7:6690313-6690363	MCF-7	breast:	n/a
45	chr7:6693334-6693384	IMR90	lung:	fetal
46	chr7:6693334-6693384	GM12878	blood:	n/a
47	chr7:6691949-6691999	ovcar-3	ovarian:	n/a
48	chr7:6691949-6691999	ProgFib	skin:	n/a
49	chr7:6694373-6694423	Hepatocyte	liver:	n/a
50	chr7:6693838-6693888	LNCaP	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6683236..6686038-chr7:6768255..6771021,2	K562	blood:
2	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
3	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
4	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
5	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:
6	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
7	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
8	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
9	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
10	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
11	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
12	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
13	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
14	chr7:6687023..6688997-chr7:6745010..6747605,2	K562	blood:
15	chr7:6682551..6684434-chr7:6694308..6696080,2	MCF-7	breast:
16	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
17	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
18	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
19	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
20	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
21	chr7:6614762..6617092-chr7:6682142..6684739,2	K562	blood:
22	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
23	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

No data

Variant related genes	Relation type
ENSG00000260054	TF binding region
ENSG00000260054	CpG island
ENSG00000164631	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000187953	chromatin interactions

Extended variants
information (count: 510 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2253869	chr7:6683454-6683455	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546918989	chr7:6683458-6683459	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs534035959	chr7:6683464-6683465	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs201525717	chr7:6683481-6683482	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs35292653	chr7:6683492-6683493	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs375564040	chr7:6683569-6683570	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs576937401	chr7:6683570-6683571	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs530071063	chr7:6683634-6683635	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs12669635	chr7:6683640-6683641	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs544064990	chr7:6683641-6683642	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs114961651	chr7:6683654-6683655	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs574447400	chr7:6683684-6683685	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs565884272	chr7:6683688-6683689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs73061333	chr7:6683697-6683698	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs140540456	chr7:6683712-6683713	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs187244794	chr7:6683714-6683715	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs557742896	chr7:6683724-6683725	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs150489163	chr7:6683737-6683738	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs546061512	chr7:6683747-6683748	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs138309611	chr7:6683748-6683749	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs555526603	chr7:6683827-6683828	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs532065808	chr7:6683843-6683844	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550083410	chr7:6683861-6683862	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs2253770	chr7:6683910-6683911	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs34751372	chr7:6683930-6683931	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs554444069	chr7:6683964-6683965	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs572603934	chr7:6683965-6683966	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs566029997	chr7:6683981-6683982	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs539860486	chr7:6683984-6683985	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs558169781	chr7:6683998-6683999	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs570636130	chr7:6684045-6684046	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs556896954	chr7:6684067-6684068	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs538188287	chr7:6684073-6684074	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs370492558	chr7:6684093-6684094	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs142774176	chr7:6684094-6684095	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs574303500	chr7:6684095-6684096	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs573651119	chr7:6684101-6684102	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs541477930	chr7:6684130-6684131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs374272202	chr7:6684175-6684176	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs553472864	chr7:6684230-6684231	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs373422643	chr7:6684231-6684232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs144939454	chr7:6684240-6684241	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs545465942	chr7:6684243-6684244	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs564136142	chr7:6684256-6684257	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs192060413	chr7:6684274-6684275	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs544132894	chr7:6684298-6684299	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs562097955	chr7:6684306-6684307	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs546104652	chr7:6684339-6684340	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs11761816	chr7:6684351-6684352	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs539896168	chr7:6684386-6684387	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6678200-6683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:6678200-6684200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:6678200-6685000	Strong transcription	NHEK	skin
5	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:6678600-6687800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:6678600-6687800	Strong transcription	Fetal Intestine Large	intestine
10	chr7:6678600-6689600	Strong transcription	Fetal Intestine Small	intestine
11	chr7:6678800-6685600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr7:6678800-6688600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:6678800-6689600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr7:6678800-6691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:6678800-6691400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:6679000-6684600	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr7:6679000-6684800	Strong transcription	A549	lung
18	chr7:6679000-6687800	Strong transcription	Fetal Stomach	stomach
19	chr7:6679000-6689200	Strong transcription	Thymus	Thymus
20	chr7:6679000-6689400	Strong transcription	Fetal Thymus	thymus
21	chr7:6679000-6689600	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:6679000-6690000	Strong transcription	Fetal Brain Female	brain
23	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
24	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
25	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
26	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
27	chr7:6679200-6690200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:6679200-6690200	Strong transcription	Lung	lung
29	chr7:6679200-6690200	Strong transcription	NHLF	lung
30	chr7:6679200-6695400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:6679400-6691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr7:6679400-6691600	Strong transcription	Liver	Liver
33	chr7:6679400-6696400	Strong transcription	Brain Hippocampus Middle	brain
34	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr7:6679600-6689200	Strong transcription	Brain Germinal Matrix	brain
36	chr7:6679600-6689400	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr7:6679600-6689600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:6679600-6693200	Strong transcription	Rectal Smooth Muscle	rectum
39	chr7:6679600-6699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:6679800-6686400	Strong transcription	GM12878-XiMat	blood
41	chr7:6679800-6687400	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr7:6679800-6689400	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr7:6679800-6689400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:6679800-6690600	Strong transcription	Fetal Muscle Leg	muscle
45	chr7:6679800-6695600	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr7:6680000-6686200	Strong transcription	Fetal Muscle Trunk	muscle
47	chr7:6680000-6686400	Strong transcription	Brain Substantia Nigra	brain
48	chr7:6680000-6689000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:6680000-6691600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr7:6680000-6692600	Strong transcription	Primary T helper cells PMA-I stimulated	--

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